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- 保存条件:
4°C, protect from light
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
343307-76-6
- 规格:
10 mM * 1 mL/5 mg/10 mg/25 mg/50 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥851.0 |
|---|---|---|---|
| 规格: | 5 mg | 产品价格: | ¥800.0 |
| 规格: | 10 mg | 产品价格: | ¥1200.0 |
| 规格: | 25 mg | 产品价格: | ¥2400.0 |
| 规格: | 50 mg | 产品价格: | ¥3800.0 |
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L48H37
CAS No. : 343307-76-6
MCE 国际站:L48H37
产品活性:L48H37 是一种化学稳定性提高了的姜黄素 (HY-N0005) 类似物。L48H37 是一种有效且特异性的髓系分化蛋白 2 (MD2) 抑制剂,抑制 LPS-TLR4/MD2 的相互作用和信号转导。L48H37 用于脓毒症或肺损伤的相关研究。
作用靶点:Toll-like Receptor (TLR)
In Vitro: L48H37 inhibits LPS-induced inflammation, particularly TNF-α and IL-6 production and gene expression in mouse macrophages.
L48H37 (0-20 µM; 24 hours) decreases the viability of A549 and H460 cells with IC50 values of 5.3 µM and 2.3 µM, respectively, which is more effective compared to curcumin in lung cancer cells. It shows a low cytotoxicity on normal human lung epithelial cells (BEAS-2B) with IC50 of 21 μM.
L48H37 (1, 2, or 4 µM; 16 hours) dose‐dependently inhibited the expression of p‐Cdc2 and Cdc2, and increases the expression of p53. It also shows increased levels of cleaved poly (ADP‐ribosyl) polymerase (PARP) and reduced levels of anti‐apoptotic protein Bcl‐2 in H460 and A549 cells.
L48H37 (4 µM; 16 hours) rapidly induces intracellular ROS levels dose-dependently as detected by increased DCF levels in H460 and A549 cells.
In Vivo: L48H37 (intraperitoneal injection; 5 mg or 10 mg/kg; once daily; 11‐day ) inhibits H460 xenograft tumor growth and exhibits anti‐tumor activity in mice.
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文献和实验5.99 5.82 5.69 5.60 5.52 5.46 5.37 5.27 5.17 5.06 4.96 4.85 6 7 6.54 5.89 5.52 5.28 5.12 4.99 4.90 4.82 4.76 4.67 4.57 4.47 4.36 4.25 4.14 7 8 6.06 5.42 5.05 4.82 4.65 4.53 4.43 4.36 4.29 4.20 4.10 4.00 3.89 3.78 3.67 8 9 5.71 5.08 4.72 4.48
悬液调整浓度至 1,500 个细胞/μl。 类器官培养 9、将冻存的 Matrigel 在 4℃ 下过夜解冻,在冰上以 7:3 的体积比将 Matrigel 与细胞悬液混合,轻轻吹打混匀避免产生气泡。 10、从 37℃ 培养箱中取出预热的 48 孔板,将 20μl 混合液接种在各孔中,注意需接种在孔的中心,避免接触侧壁。 11、将 48 孔板倒置放入 37℃,5%CO2 的培养箱中孵育 10min,使 Matrigel 固化。 12、向每个孔中缓慢滴加 250μl 预热的 OCO (Ovarian
的 BMDMs 细胞的 pull down 蛋白;G-J:IP 和 WB 分析 EST12 处理的 BMDMs 细胞;K:共聚焦显微镜分析 EST12 处理后的 WT 和 RACK1−/−腹腔巨噬细胞;L:IP 和 IB 分析 EST12 处理或未预处理的腹腔巨噬细胞。 将编码 WT 泛素(H-Ub)、突变 H-Ub(K48)和 H-Ub(K63)质粒转染至 RAW264.7 细胞,通过 IP 和 WB 实验,推测 EST12 介导了 K48 连接的 NLRP3 去泛素化(图 4E)。WB 分析 EST
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